ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.14637A>C (p.Gln4879His)

dbSNP: rs1553341953
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000618580 SCV000736073 uncertain significance Cardiovascular phenotype 2017-10-26 criteria provided, single submitter clinical testing The p.Q4879H variant (also known as c.14637A>C), located in coding exon 102 of the RYR2 gene, results from an A to C substitution at nucleotide position 14637. The glutamine at codon 4879 is replaced by histidine, an amino acid with highly similar properties. This amino acid position is highly conserved in available vertebrate species. In addition, this alteration is predicted to be deleterious by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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